Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518681
rs1057518681
PUF60 ; SCRIB
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518843
rs1057518843
GALC
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518845
rs1057518845
SOX5 ; LOC105369696
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518848
rs1057518848
TCF4
CATTG 0.700 CausalMutation CLINVAR

dbSNP: rs1057518926
rs1057518926
FOXP1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519429
rs1057519429
CACNA1A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1057519436
rs1057519436
DHX30
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057519443
rs1057519443
MPP4
G 0.700 CausalMutation CLINVAR

dbSNP: rs1060499733
rs1060499733
DHX30
G 0.700 CausalMutation CLINVAR

dbSNP: rs1064796765
rs1064796765
DYNC1H1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1085307993
rs1085307993
GABRB2
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1163944538
rs1163944538
TMEM94
GA 0.700 CausalMutation CLINVAR

dbSNP: rs1172486173
rs1172486173
QARS1 ; MIR6890
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1276519904
rs1276519904
H3-3A
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1325394060
rs1325394060
HUWE1
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1352010373
rs1352010373
TMEM94
C 0.700 CausalMutation CLINVAR

dbSNP: rs137854539
rs137854539
GNAS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs139751598
rs139751598
PYCR1
T 0.700 CausalMutation CLINVAR

dbSNP: rs148677674
rs148677674
LZTR1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1553196101
rs1553196101
CDC42
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553196134
rs1553196134
CDC42
T 0.700 CausalMutation CLINVAR

dbSNP: rs1553212868
rs1553212868
POGZ
C 0.700 CausalMutation CLINVAR

dbSNP: rs1553621496
rs1553621496
UNC80
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1554888939
rs1554888939
EHMT1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1555247805
rs1555247805
MED13L
C 0.700 CausalMutation CLINVAR